A simple approach for the synthesis of 2,6-diaryl-4-oxo-3,4- dihydropyrimidine-5-carbonitriles

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Abstract

A concise, facile and straightforward synthesis of 2,6-diaryl-4-oxo-3,4- dihydropyrimidine-5-carbonitriles 12a-h is reported. The reaction for this preparation involves the condensation of ethyl α-cyanocinnamate and its para substituted analogs 8a-e with arylamidines 9a-d under very mild conditions. A probable mechanism of 12a-h from 11a-h is proposed. A preliminary pharmacological evaluation of compounds 12c, 12d, 12f e 12h has shown that these compounds possess analgesic activity.

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Mendonça, F. J. B., Dos Anjos, J. V., Falcão, E. P. S., De Melo, S. J., & Srivastava, R. M. (2005). A simple approach for the synthesis of 2,6-diaryl-4-oxo-3,4- dihydropyrimidine-5-carbonitriles. Heterocyclic Communications, 11(6), 479–484. https://doi.org/10.1515/hc.2005.11.6.479

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